FDA 510(k)

SKYTRON MODEL 1100 AND MODEL 142

K-Number: K900290 · 1990-02-20

ApplicantSkytron, Div. the Kmw Group, Inc.

Decision Date1990-02-20

Product CodeJEA

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SKYTRON MODEL 1100 AND MODEL 142 is the device name listed in this FDA 510(k) record. The listed applicant is Skytron, Div. the Kmw Group, Inc.. It received FDA 510(k) clearance on 1990-02-20 under 510(k) number K900290. The device is classified under product code JEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKYTRON MODEL 1100 AND MODEL 142?

SKYTRON MODEL 1100 AND MODEL 142 is a medical device that received FDA 510(k) clearance on 1990-02-20. The listed applicant is Skytron, Div. the Kmw Group, Inc.. The 510(k) number is K900290.

When did SKYTRON MODEL 1100 AND MODEL 142 receive FDA 510(k) clearance?

SKYTRON MODEL 1100 AND MODEL 142 received FDA 510(k) clearance on 1990-02-20, under 510(k) number K900290.

Who is the listed applicant for SKYTRON MODEL 1100 AND MODEL 142?

The FDA 510(k) record lists Skytron, Div. the Kmw Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKYTRON MODEL 1100 AND MODEL 142?

The FDA product code for SKYTRON MODEL 1100 AND MODEL 142 is JEA.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.